A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565166



Internal ID20938237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157070361..157070760hg38UCSC Ensembl
chr7:156863055..156863454hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565166
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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